GxP Clinical Systems Lead — Remote/Hybrid

Structure Therapeutics Inc.; South San Francisco (CA); Hybrid; USD 166,000 - 209,000; Full time

Benefits offered by this job

Annual bonus

Equity / stock options

Medical, dental, vision insurance

401k match

Unlimited PTO

Winter shutdown holidays

Job summary

Structure Therapeutics Inc. is seeking a Senior Manager, Clinical Business Systems to own and govern GxP-regulated platforms (Veeva Vault QMS, LMS, CTMS, eTMF; Box; DocuSign) and to drive adoption, validation, and continuous improvement.

You will collaborate across Clinical, Quality, Regulatory, and IT teams to ensure inspection readiness and scalable processes. The role combines hands-on administration with vendor management, change control, and documentation.

Qualifications

• Bachelor's degree in Computer Science, Life Sciences or related field recommended.
• 8+ years of experience supporting GxP-regulated systems in pharma/biotech/med device.
• Hands-on administration of Veeva Vault, Box for Life Sciences, DocuSign, SAS.
• Knowledge of 21 CFR Part 11, EU Annex 11, GAMP 5, ICH guidelines, data integrity.
• Experience leading cross-functional tech initiatives and vendor relationships.

Responsibilities

• Serve as product owner for assigned GxP applications; drive lifecycle management and adoption.
• Manage day-to-day system administration: provisioning, roles, configuration, maintenance.
• Coordinate releases, upgrades and changes with vendors; ensure change control compliance.
• Support validation activities and maintain documentation for validated state.
• Partner with stakeholders to prioritize enhancements and maintain roadmaps.

Skills

GxP admin

Vendor management

Cross-functional

Documentation

Communication

Problem solving

Agile/ITIL

Education

Bachelor's degree

Tools

Veeva Vault

Box for Life Sciences

DocuSign

SAS

Job description

Structure Therapeutics Inc. is seeking a Senior Manager, Clinical Business Systems to own and govern GxP-regulated platforms (Veeva Vault QMS, LMS, CTMS, eTMF; Box; DocuSign) and to drive adoption, validation, and continuous improvement.

You will collaborate across Clinical, Quality, Regulatory, and IT teams to ensure inspection readiness and scalable processes. The role combines hands-on administration with vendor management, change control, and documentation.